Rigter H, Jensen R A, Martinez J L, Messing R B, Vasquez B J, Liang K C, McGaugh J L
Proc Natl Acad Sci U S A. 1980 Jun;77(6):3729-32. doi: 10.1073/pnas.77.6.3729.
Leu[Enkephalin (400.0 micrograms/kg) and the enkephalin analog [DAla,DLeu]enkephalin (0.4, 4.0, and 40.0 micrograms/kg) were intraperitoneally administered to rats 5 min before they were trained on aversively motivated tasks. The peptides impaired acquisition of a one-way active avoidance response, facilitated acquisition of an inhibitory avoidance response, and had no effect on acquisition of a swim-escape response. The data indicate that the enkephalin effects are not mediated through actions on locomotor activity, pain perception or reactivity, or light sensitivity. Rather, we suggest that [Leu]enkephalin and its analog strengthen the tendency of rats to suppress behavior in the presence of cues previously associated with aversive stimulation. This effect may be due to an enkephalin-induced increase in fear or arousal. The enkephalin effect on behavior was obtained at low doses and was observed within a few minutes after administration. These findings are consistent with the interpretation that enkephalin effects may be initiated at a peripheral site.
亮氨酸脑啡肽(400.0微克/千克)和脑啡肽类似物[D - 丙氨酸,D - 亮氨酸]脑啡肽(0.4、4.0和40.0微克/千克)在大鼠接受厌恶性动机任务训练前5分钟腹腔注射。这些肽损害了单向主动回避反应的习得,促进了抑制性回避反应的习得,并且对游泳逃避反应的习得没有影响。数据表明,脑啡肽的作用不是通过对运动活动、疼痛感知或反应性或光敏感性的作用来介导的。相反,我们认为亮氨酸脑啡肽及其类似物增强了大鼠在存在先前与厌恶性刺激相关的线索时抑制行为的倾向。这种作用可能是由于脑啡肽诱导的恐惧或觉醒增加。脑啡肽对行为的影响在低剂量时即可获得,并且在给药后几分钟内即可观察到。这些发现与脑啡肽作用可能在外周部位启动的解释一致。